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List of works by Andrew Tym Hattersley

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Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

scientific article
A common variation in deiodinase 1 gene DIO1 is associated with the relative levels of free thyroxine and triiodothyronine

scientific article published on 20 May 2008
Genetic regulation of birth weight and fasting glucose by a common polymorphism in the islet cell promoter of the glucokinase gene

scientific article published in February 2005
Insights into the structure and regulation of glucokinase from a novel mutation (V62M), which causes maturity-onset diabetes of the young

scientific article
Variation in the calpain-10 gene affects blood glucose levels in the British population

scientific article published in January 2002
Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

scientific article published on 3 January 2018
Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus

scientific article
Permanent neonatal diabetes due to paternal germline mosaicism for an activating mutation of the KCNJ11 Gene encoding the Kir6.2 subunit of the beta-cell potassium adenosine triphosphate channel

scientific article
Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment

scientific article
Paradoxical lower serum triglyceride levels and higher type 2 diabetes mellitus susceptibility in obese individuals with the PNPLA3 148M variant

scientific article
Fetal thyroid hormone level at birth is associated with fetal growth

scientific article
The Exeter Family Study of Childhood Health (EFSOCH): study protocol and methodology

scientific article published in March 2006
Genetic Evidence for a Link Between Favorable Adiposity and Lower Risk of Type 2 Diabetes, Hypertension, and Heart Disease

scientific article published on 26 April 2016
Use of HbA1c in the identification of patients with hyperglycaemia caused by a glucokinase mutation: observational case control studies

scientific article
Triglyceride associated polymorphisms of the APOA5 gene have very different allele frequencies in Pune, India compared to Europeans

scientific article
Most People With Long-Duration Type 1 Diabetes in a Large Population-Based Study Are Insulin Microsecretors

scientific article published on December 17, 2014
The diabetic phenotype in HNF4A mutation carriers is moderated by the expression of HNF4A isoforms from the P1 promoter during fetal development

scientific article
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes

scientific article
Stability and reproducibility of a single-sample urinary C-peptide/creatinine ratio and its correlation with 24-h urinary C-peptide

scientific article published on 27 August 2009
Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia

scientific article published on 8 November 2011
Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes

scholarly article
Markers of β-Cell Failure Predict Poor Glycemic Response to GLP-1 Receptor Agonist Therapy in Type 2 Diabetes

scientific article published on 04 August 2015
Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes

scientific article
Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

scientific article published on 26 August 2008
Evidence of genetic regulation of fetal longitudinal growth

scientific article published on 8 August 2005
Beta-cell dysfunction, insulin sensitivity, and glycosuria precede diabetes in hepatocyte nuclear factor-1alpha mutation carriers

scientific article published in July 2005
The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

scientific article
Urine C-peptide creatinine ratio is a noninvasive alternative to the mixed-meal tolerance test in children and adults with type 1 diabetes

scientific article
GATA4 mutations are a cause of neonatal and childhood-onset diabetes.

scientific article published on 2 April 2014
Measurement of cord insulin and insulin-related peptides suggests that girls are more insulin resistant than boys at birth

scientific article published on 2 May 2007
The 0.1% of the population with glucokinase monogenic diabetes can be recognized by clinical characteristics in pregnancy: the Atlantic Diabetes in Pregnancy cohort

scientific article published on 18 February 2014
A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young: Evidence for Further Genetic Heterogeneity

article
Distinct molecular and morphogenetic properties of mutations in the human HNF1beta gene that lead to defective kidney development

scientific article published on 01 August 2003
Identifying hepatic nuclear factor 1alpha mutations in children and young adults with a clinical diagnosis of type 1 diabetes

scientific article
Lower Circulating B12 Is Associated with Higher Obesity and Insulin Resistance during Pregnancy in a Non-Diabetic White British Population

scientific article
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry

article by Sara Pulit et al published 1 January 2019 in Human Molecular Genetics
Dietary energy density affects fat mass in early adolescence and is not modified by FTO variants

scientific article
'I don't feel like a diabetic any more': the impact of stopping insulin in patients with maturity onset diabetes of the young following genetic testing

scientific article
Genetic evidence of assortative mating in humans

scholarly article
The impact of maternal glycemia and obesity on early postnatal growth in a nondiabetic Caucasian population

scientific article published on 24 January 2007
Population-Based Assessment of a Biomarker-Based Screening Pathway to Aid Diagnosis of Monogenic Diabetes in Young-Onset Patients

scientific article published on 12 July 2017
Underlying genetic models of inheritance in established type 2 diabetes associations

scientific article published on 14 July 2009
Large-scale studies of the association between variation at the TNF/LTA locus and susceptibility to type 2 diabetes.

scientific article
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes

scientific article
A powerful approach to sub-phenotype analysis in population-based genetic association studies

scientific article
Association and haplotype analysis of the insulin-degrading enzyme (IDE) gene, a strong positional and biological candidate for type 2 diabetes susceptibility

scientific article published in May 2003
Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations

scientific article published on 15 July 2010
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

scientific article published on 17 September 2009
Messenger RNA transcripts of the hepatocyte nuclear factor-1alpha gene containing premature termination codons are subject to nonsense-mediated decay

scientific article published on February 2004
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNALeu A to G mutation11The authors have no proprietary interest in the development or marketing of any device or medica

article

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